The CoVID-TE risk assessment model for venous thromboembolism in hospitalized patients with cancer and COVID-19.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
10 2021
Historique:
revised: 24 06 2021
received: 01 06 2021
accepted: 12 07 2021
pubmed: 15 7 2021
medline: 29 9 2021
entrez: 14 7 2021
Statut: ppublish

Résumé

Hospitalized patients with COVID-19 have increased risks of venous (VTE) and arterial thromboembolism (ATE). Active cancer diagnosis and treatment are well-known risk factors; however, a risk assessment model (RAM) for VTE in patients with both cancer and COVID-19 is lacking. To assess the incidence of and risk factors for thrombosis in hospitalized patients with cancer and COVID-19. Among patients with cancer in the COVID-19 and Cancer Consortium registry (CCC19) cohort study, we assessed the incidence of VTE and ATE within 90 days of COVID-19-associated hospitalization. A multivariable logistic regression model specifically for VTE was built using a priori determined clinical risk factors. A simplified RAM was derived and internally validated using bootstrap. From March 17, 2020 to November 30, 2020, 2804 hospitalized patients were analyzed. The incidence of VTE and ATE was 7.6% and 3.9%, respectively. The incidence of VTE, but not ATE, was higher in patients receiving recent anti-cancer therapy. A simplified RAM for VTE was derived and named CoVID-TE (Cancer subtype high to very-high risk by original Khorana score +1, VTE history +2, ICU admission +2, D-dimer elevation +1, recent systemic anti-cancer Therapy +1, and non-Hispanic Ethnicity +1). The RAM stratified patients into two cohorts (low-risk, 0-2 points, n = 1423 vs. high-risk, 3+ points, n = 1034) where VTE occurred in 4.1% low-risk and 11.3% high-risk patients (c statistic 0.67, 95% confidence interval 0.63-0.71). The RAM performed similarly well in subgroups of patients not on anticoagulant prior to admission and moderately ill patients not requiring direct ICU admission. Hospitalized patients with cancer and COVID-19 have elevated thrombotic risks. The CoVID-TE RAM for VTE prediction may help real-time data-driven decisions in this vulnerable population.

Sections du résumé

BACKGROUND
Hospitalized patients with COVID-19 have increased risks of venous (VTE) and arterial thromboembolism (ATE). Active cancer diagnosis and treatment are well-known risk factors; however, a risk assessment model (RAM) for VTE in patients with both cancer and COVID-19 is lacking.
OBJECTIVES
To assess the incidence of and risk factors for thrombosis in hospitalized patients with cancer and COVID-19.
METHODS
Among patients with cancer in the COVID-19 and Cancer Consortium registry (CCC19) cohort study, we assessed the incidence of VTE and ATE within 90 days of COVID-19-associated hospitalization. A multivariable logistic regression model specifically for VTE was built using a priori determined clinical risk factors. A simplified RAM was derived and internally validated using bootstrap.
RESULTS
From March 17, 2020 to November 30, 2020, 2804 hospitalized patients were analyzed. The incidence of VTE and ATE was 7.6% and 3.9%, respectively. The incidence of VTE, but not ATE, was higher in patients receiving recent anti-cancer therapy. A simplified RAM for VTE was derived and named CoVID-TE (Cancer subtype high to very-high risk by original Khorana score +1, VTE history +2, ICU admission +2, D-dimer elevation +1, recent systemic anti-cancer Therapy +1, and non-Hispanic Ethnicity +1). The RAM stratified patients into two cohorts (low-risk, 0-2 points, n = 1423 vs. high-risk, 3+ points, n = 1034) where VTE occurred in 4.1% low-risk and 11.3% high-risk patients (c statistic 0.67, 95% confidence interval 0.63-0.71). The RAM performed similarly well in subgroups of patients not on anticoagulant prior to admission and moderately ill patients not requiring direct ICU admission.
CONCLUSIONS
Hospitalized patients with cancer and COVID-19 have elevated thrombotic risks. The CoVID-TE RAM for VTE prediction may help real-time data-driven decisions in this vulnerable population.

Identifiants

pubmed: 34260813
doi: 10.1111/jth.15463
pmc: PMC8420489
pii: S1538-7836(22)02157-2
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2522-2532

Subventions

Organisme : NCI NIH HHS
ID : P30 CA068485
Pays : United States
Organisme : National Hemophilia Foundation
ID : Shire Clinical Fellowship Award
Organisme : Hemostasis and Thrombosis Research Society
ID : Mentored Research Award
Organisme : Cancer Prevention and Research Institute of Texas
ID : RR190104

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis.

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Auteurs

Ang Li (A)

Section of Hematology-Oncology, Baylor College of Medicine, Houston, Texas, USA.

Nicole M Kuderer (NM)

Advanced Cancer Research Group, Seattle, Washington, USA.

Chih-Yuan Hsu (CY)

Department of Biomedical Informatics, Vanderbilt University, Nashville, Tennessee, USA.

Yu Shyr (Y)

Department of Biomedical Informatics, Vanderbilt University, Nashville, Tennessee, USA.

Jeremy L Warner (JL)

Department of Biomedical Informatics, Vanderbilt University, Nashville, Tennessee, USA.
Department of Medicine, Division of Hematology/Oncology, Vanderbilt University, Nashville, Tennessee, USA.

Dimpy P Shah (DP)

Mays Cancer Center at UT Health San Antonio MD Anderson Cancer Center, San Antonio, Texas, USA.

Vaibhav Kumar (V)

Section of Hematology-Oncology, University of North Carolina, Chapel Hill, North Carolina, USA.

Surbhi Shah (S)

Division of Hematology, Oncology, and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA.

Amit A Kulkarni (AA)

Division of Hematology, Oncology, and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA.

Julie Fu (J)

Hematology Oncology, Tufts Medical Center Cancer Center, Boston & Stoneham, Massachusetts, USA.

Shuchi Gulati (S)

Division of Hematology/Oncology, University of Cincinnati, Cincinnati, Ohio, USA.

Rebecca L Zon (RL)

Division of Hematology, Brigham and Women's Hospital Boston, Boston, Massachusetts, USA.

Monica Li (M)

School of Medicine, Baylor College of Medicine, Houston, Texas, USA.

Aakash Desai (A)

Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Pamela C Egan (PC)

Brown University and Lifespan Cancer Institute, Providence, Rhode Island, USA.

Ziad Bakouny (Z)

Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Devendra Kc (D)

Hartford HealthCare Cancer Institute, Hartford, Connecticutt, USA.

Clara Hwang (C)

Henry Ford Cancer Institute, Henry Ford Hospital, Detroit, Michigan, USA.

Imo J Akpan (IJ)

Herbert Irving Comprehensive Cancer Center at Columbia University, New York, New York, USA.

Rana R McKay (RR)

Moores Cancer Center at the University of California, San Diego, California, USA.

Jennifer Girard (J)

University of Michigan Rogel Cancer Center, Ann Arbor, Michigan, USA.

Andrew L Schmidt (AL)

Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Balazs Halmos (B)

Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York, USA.

Michael A Thompson (MA)

Aurora Cancer Care, Advocate Aurora Health, Milwaukee, Wisconsin, USA.

Jaymin M Patel (JM)

Beth Israel Deaconess Medical Center (BIDMC), Boston, Massachusetts, USA.

Nathan A Pennell (NA)

Cleveland Clinic, Cleveland, Ohio, USA.

Solange Peters (S)

Lausanne University Hospital, Lausanne, Switzerland.

Amro Elshoury (A)

Leukemia Service, Department of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.

Gilbero de Lima Lopes (G)

Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida, USA.

Daniel G Stover (DG)

Ohio State University Comprehensive Cancer Center, Columbus, Ohio, USA.

Petros Grivas (P)

University of Washington, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, Seattle, Washington, USA.

Brian I Rini (BI)

Department of Medicine, Division of Hematology/Oncology, Vanderbilt University, Nashville, Tennessee, USA.

Corrie A Painter (CA)

Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.

Sanjay Mishra (S)

Department of Medicine, Division of Hematology/Oncology, Vanderbilt University, Nashville, Tennessee, USA.

Jean M Connors (JM)

Division of Hematology, Brigham and Women's Hospital Boston, Boston, Massachusetts, USA.

Gary H Lyman (GH)

University of Washington, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, Seattle, Washington, USA.

Rachel P Rosovsky (RP)

Division of Hematology/Oncology, Massachusetts General Hospital, Boston, Massachusetts, USA.

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